Clinical Trial Manager

Role: Clinical Trial Manager (CTM) overseeing operational execution of assigned clinical trials in biopharma, from planning to closeout. Objectives include ensuring compliance, quality, and timely delivery of studies, managing CROs and external vendors, and maintaining regulatory and GCP standards. Responsibilities encompass study start-up, site management, regulatory documentation, vendor oversight, data review, risk mitigation, and cross-functional coordination across clinical, data, and regulatory teams. The CTM leads study team meetings, manages budgets, develops timelines, and ensures audit readiness. Qualifications: Bachelor's in health, biological sciences, or related field; minimum 8 years of clinical study management experience, including at least 5 years as a lead or project manager; prior CRO/vendor management experience; experience across phase 1-4, with oncology experience preferred. High-value specifics include managing trials in oncology, ensuring compliance with GCP, ICH, and global regulations, and proficiency in clinical operations, data review, and site management. The role may be hybrid (Norwood, MA) or remote with travel to US or UK, depending on location.